Job Title: Senior Research Associate – Biopharmaceutics (BPH)
Location: Bangalore, Karnataka, India
Employment Type: Full-Time, Permanent
Department: Biopharmaceutics (BPH) / Dedicated Centre
Syngene International Ltd., established in 1993, is a global contract research, development, and manufacturing organization (CRDMO) delivering integrated scientific services across pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Syngene collaborates with leading global clients, including Bristol-Myers Squibb, Amgen, GSK, Merck KGaA, and Herbalife, to accelerate research and development, reduce time-to-market, and enhance innovation efficiency.
The Senior Research Associate (BPH) will conduct pre-formulation and phase-appropriate formulation development studies to support pre-clinical and clinical projects. The role involves evaluating new chemical entities (NCEs), assisting in oral dosage form development, and contributing to data analysis and scientific reporting.
Conduct pre-formulation studies to evaluate physicochemical properties of NCEs.
Perform solid-state characterization and analytical assessments to support formulation development.
Assist in the development of oral drug products (solutions, suspensions, tablets, capsules) for pre-clinical PK/PD and toxicology studies.
Conduct feasibility and formulation studies, ensuring alignment with study objectives and regulatory requirements.
Accurately record, summarize, and present experimental results; assist in drafting scientific and technical reports.
Operate and maintain analytical instruments and software used in drug discovery and formulation development.
Collaborate with cross-functional teams including PK/PD, toxicology, medicinal chemistry, and analytical R&D.
Occasionally liaise with clients to provide project updates and technical insights.
M. Pharm or M.S. in Pharmaceutics / Pharmaceutical Chemistry.
2–5 years of experience in pre-formulation, formulation development, or pharmaceutical R&D is preferred.
Expertise in physicochemical property assessment, pre-formulation studies, analytical chemistry, formulation development, and stability studies.
Proficient in data interpretation, solid-state characterization, and laboratory instrumentation.
Working knowledge of Microsoft Office and scientific software tools.
Team-oriented and ready to learn and collaborate across functions.
Strong communication, presentation, and scientific writing skills.
Ability to work effectively in a cross-functional, multidisciplinary environment.
Internal collaboration with PK/PD, toxicology, medicinal chemistry, and analytical R&D teams.
Occasional external interaction with clients on discovery and development pharmaceutics.
Contribute to innovative drug development projects for global clients.
Work in a dynamic, collaborative, and globally recognized R&D environment.
Gain exposure to cutting-edge formulation development techniques and scientific tools.
Opportunity to enhance technical expertise and professional growth in a leading CRDMO.
Syngene International Ltd. is committed to providing equal employment opportunities (EEO) for all candidates, regardless of age, gender, race, disability, religion, sexual orientation, or any other legally protected characteristic. Reasonable accommodations are provided for qualified individuals with disabilities.
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